Toxicity of beauvericin on porcine oocyte maturation and preimplantation embryo development
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作者:
Schoevers, Eric J.
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Univ Utrecht, Fac Vet Med, Dept Farm Anim Hlth, Yalelaan 104, NL-3584 CM Utrecht, NetherlandsUniv Utrecht, Fac Vet Med, Dept Farm Anim Hlth, Yalelaan 104, NL-3584 CM Utrecht, Netherlands
Schoevers, Eric J.
[1
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Santos, Regiane R.
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Univ Utrecht, Fac Vet Med, Inst Risk Assessment Sci, Div Vet Pharmacol Pharmacotherapy & Toxicol, Yalelaan 104, NL-3584 CM Utrecht, NetherlandsUniv Utrecht, Fac Vet Med, Dept Farm Anim Hlth, Yalelaan 104, NL-3584 CM Utrecht, Netherlands
Santos, Regiane R.
[2
]
Fink-Gremmels, Johanna
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Univ Utrecht, Fac Vet Med, Inst Risk Assessment Sci, Div Vet Pharmacol Pharmacotherapy & Toxicol, Yalelaan 104, NL-3584 CM Utrecht, NetherlandsUniv Utrecht, Fac Vet Med, Dept Farm Anim Hlth, Yalelaan 104, NL-3584 CM Utrecht, Netherlands
Fink-Gremmels, Johanna
[2
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Roelen, Bernard A. J.
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Univ Utrecht, Fac Vet Med, Dept Farm Anim Hlth, Yalelaan 104, NL-3584 CM Utrecht, NetherlandsUniv Utrecht, Fac Vet Med, Dept Farm Anim Hlth, Yalelaan 104, NL-3584 CM Utrecht, Netherlands
Roelen, Bernard A. J.
[1
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机构:
[1] Univ Utrecht, Fac Vet Med, Dept Farm Anim Hlth, Yalelaan 104, NL-3584 CM Utrecht, Netherlands
[2] Univ Utrecht, Fac Vet Med, Inst Risk Assessment Sci, Div Vet Pharmacol Pharmacotherapy & Toxicol, Yalelaan 104, NL-3584 CM Utrecht, Netherlands
Beauvericin (BEA) is one of many toxins produced by Fusarium species that contaminate feed materials. The aim of this study was to assess its effects on porcine oocyte maturation and preimplantation embryo development. Cumulus-oocyte-complexes and developing embryos were exposed to BEA and cultured until the blastocyst stage. Cumulus cells, oocytes and embryos were examined for viability, progesterone synthesis, multidrug resistance protein (MDR1), ATP content and gene expression related to MDR1 function, oxidative phosphorylation, steroidogenesis and apoptosis. BEA was toxic in embryos, oocytes and cumulus cells at concentrations exceeding 0.5 mu M, and embryos were most vulnerable after the four-cell stage. Since BEA exerted different effects in embryos, oocytes and cumulus cells, the toxic mechanism is suggested to involve different pathways. Currently there are no consistent data on adverse effects of BEA in pig farms. (C) 2016 The Authors. Published by Elsevier Inc. This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).